<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-21T23:54:26Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/5242" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/5242</identifier><datestamp>2024-09-27T09:14:55Z</datestamp><setSpec>com_20.500.12105_19604</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19605</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">de Lucas, Beatriz</subfield>
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      <subfield code="a">Bernal, Aurora</subfield>
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      <subfield code="a">Perez, Laura M.</subfield>
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      <subfield code="a">San Martin, Nuria</subfield>
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      <subfield code="a">Galvez, Beatriz G.</subfield>
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      <subfield code="c">2016</subfield>
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      <subfield code="a">Mesenchymal precursors (MPs) present some advantageous features, such as differentiation and migration, which make them promising candidates for cell therapy. A better understanding of MP migration characteristics would aid the development of cell delivery protocols. Traditionally, cell migration is thought to occur only through the formation of lamellipodia. More recently, contractility-driven bleb formation has emerged as an alternative mechanism of motility. Here we report that MPs derived from different tissues present spontaneously dynamic cytoplasmic projections in sub-confluent culture, which appear as a combination of lamellipodia with blebs in the leading edge. Upon initial seeding, however, only bleb structures could be observed. Immunofluorescence revealed the presence of pERM, RhoA and F-actin during the blebbing process. Results from migration assays in the presence of blebbistatin, a myosin II inhibitor, showed that bleb formation correlated with migratory capacity, suggesting a functional role for blebs in migration. Bleb formation might be a useful mechanism to improve cell migration in cellular therapy protocols.</subfield>
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      <subfield code="a">PLoS One. 2016; 11(3):e0150004</subfield>
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      <subfield code="a">26930466</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/5242</subfield>
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      <subfield code="a">STEM-CELLS</subfield>
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      <subfield code="a">CARDIAC MESOANGIOBLASTS</subfield>
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      <subfield code="a">AMEBOID MIGRATION</subfield>
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      <subfield code="a">SKELETAL-MUSCLE</subfield>
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      <subfield code="a">INVASION</subfield>
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      <subfield code="a">BLEBS</subfield>
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      <subfield code="a">LAMELLIPODIA</subfield>
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      <subfield code="a">MECHANICS</subfield>
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      <subfield code="a">Membrane Blebbing Is Required for Mesenchymal Precursor Migration</subfield>
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